DE607291C - Production of soluble compounds of sulfamic acid with mercury and alkali metals - Google Patents

Production of soluble compounds of sulfamic acid with mercury and alkali metals

Info

Publication number
DE607291C
DE607291C DEK132189D DEK0132189D DE607291C DE 607291 C DE607291 C DE 607291C DE K132189 D DEK132189 D DE K132189D DE K0132189 D DEK0132189 D DE K0132189D DE 607291 C DE607291 C DE 607291C
Authority
DE
Germany
Prior art keywords
mercury
sulfamic acid
alkali
production
acid
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
DEK132189D
Other languages
German (de)
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
GEORG SCHROETER DR
Original Assignee
GEORG SCHROETER DR
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by GEORG SCHROETER DR filed Critical GEORG SCHROETER DR
Priority to DEK132189D priority Critical patent/DE607291C/en
Application granted granted Critical
Publication of DE607291C publication Critical patent/DE607291C/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B21/00Nitrogen; Compounds thereof
    • C01B21/082Compounds containing nitrogen and non-metals and optionally metals
    • C01B21/087Compounds containing nitrogen and non-metals and optionally metals containing one or more hydrogen atoms
    • C01B21/093Compounds containing nitrogen and non-metals and optionally metals containing one or more hydrogen atoms containing also one or more sulfur atoms
    • C01B21/0935Imidodisulfonic acid; Nitrilotrisulfonic acid; Salts thereof
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B21/00Nitrogen; Compounds thereof
    • C01B21/082Compounds containing nitrogen and non-metals and optionally metals
    • C01B21/087Compounds containing nitrogen and non-metals and optionally metals containing one or more hydrogen atoms
    • C01B21/093Compounds containing nitrogen and non-metals and optionally metals containing one or more hydrogen atoms containing also one or more sulfur atoms
    • C01B21/096Amidosulfonic acid; Salts thereof

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

Herstellung löslicher Verbindungen der Sulfamidsäure mit Quecksilber und Alkalimetallen Es ist bekannt, Verbindungen der Sulfamidsäure mit Quecksilber und Alkalimetallen dadureh herzustellen, daß man eine wäßrige Lösung von Sulfamidsäure mit Alikalihydroxyden und einer wasserlöslichen Quecksilberverbindung versetzt. Nach einiger Zeit scheiden sich Kristalle von der Zusammensetzung Hg N S O, Me - H20 aus. Die Ausscheidung brauchst jedoch recht lange Zeit.Production of soluble compounds of sulphamic acid with mercury and alkali metals It is known compounds of sulfamic acid with mercury and alkali metals can be prepared by using an aqueous solution of sulfamic acid mixed with alkali hydroxides and a water-soluble mercury compound. After a while, crystals separate from the composition Hg N S O, Me - H20 off. However, elimination takes a long time.

Es wurde gefunden, daß sich oxymercurisulfamidsaure Salze der Alkalien von dem Typus HO-Hg-NH-S0,-Me-xH20 in fast quantitativer Ausbeute gewinnen lassen, wenn man wäßrige Lösungen von Sulfamidsäure, Alkahhydroxyden und einer löslichen Quecksilberverbindung mit einem Alkohol versetzt, wobei die Mengenverhältnisse zweckmäßig so gewählt werden, daß auf i Mol Sulfamidsäure 3 Mole eines Alkali= hydroxydes und i Mol einer Quecksilberverbindung zur Verwendung kommen. Durch Zugabe von Alkohol oder durch Einlaufenlassen der w äßrigen Lösung in Alkohol werden die oxymercuriamidosulfonsauren Salze der Alkalien fast quantitativ gefällt. Als Alkohol kann Methyl-, Äthyl- oder ein höhefrer Alkohol dieser Reihe genommen werden. Die Verwendung eines höheren homologen Alkohols, z. B. Propylalkohol; empfiehlt sich insbesondere bei der Fällung des Lithiumsalzes, das in wäßrigem Methylalkohol merklich löslich ist. Die Alkalisalze der Oxymercurisulfamidsäure sind in Wasser leicht löslich. Bei längerem Stehen treten jedoch leicht Trübungen auf. Wie weiter gefunden wurde, lassen sich schon durch geringe Zusätze von löslichen Alkalisalzen, z. B. Salzen der Halogenwasserstoffsäure, der Phosphorsäure, der Rhodanwasserstoffsäure, der Kohlensäure oder auch von Alkalihydroxyden diese Trübungen ganz vermeiden. Ausführungsbeispiele i. 97 g reine Sulfamidsäure, i 7o g Kaliumhydroxyd und 271 g Quecksilberchlorid werden in Wasser gelöst und die klare Lösung in etwa die Hälfte ihres Volumens Methy l-oder Äthylalkohol eingerührt. Der sofort entstehende weiße und pulverige Niederschlag wird abgenutscht und mit Alkohol gewaschen. Die Ausbeute an oxymercurisulfamids-aurem Kalium von der Zusammensetzung H O - I-1- -NH - S OBK - H20 beträgt 36o g. Das Salz ist in, Wasser sehr leicht löslich und verliert beim Trocknen im Vakuum bei ioo bis iio° i Mol Wasser.It has been found that oxymercuric sulfamic acid salts of alkalis from the type HO-Hg-NH-S0, -Me-xH20 can be obtained in almost quantitative yield, when using aqueous solutions of sulfamic acid, alkahydroxides and a soluble one An alcohol is added to the mercury compound, the proportions being expedient be chosen so that 3 moles of an alkali hydroxide and 1 mole of sulfamic acid i mole of a mercury compound are used. By adding alcohol or by running the aqueous solution into alcohol, the oxymercuriamidosulfonic acids become Salts of alkalis precipitated almost quantitatively. The alcohol can be methyl, ethyl or a higher alcohol of this range can be taken. The use of a higher homologous alcohol, e.g. B. propyl alcohol; is particularly recommended for precipitation the lithium salt, which is appreciably soluble in aqueous methyl alcohol. The alkali salts of oxymercuric sulfamic acid are easily soluble in water. Kick when standing for a long time however, slight opacities. How it was found further can already be seen small additions of soluble alkali salts, e.g. B. Salts of hydrohalic acid, of phosphoric acid, hydrofluoric acid, carbonic acid or alkali hydroxides avoid these opacities entirely. Embodiments i. 97 g pure sulfamic acid, i 70 g of potassium hydroxide and 271 g of mercury chloride are dissolved in water and the Clear solution stirred in methyl or ethyl alcohol in about half of its volume. The immediately resulting white and powdery precipitate is suction filtered and with Alcohol washed. The yield of oxymercuric sulfamic acid potassium from the composition H O - I-1- -NH - S OBK - H20 is 36o g. The salt is very light in, water soluble and loses on drying in vacuo at 100 to 100 moles of water.

a: In gleicher Weise wie in Beispiel i wird auch das Natriumsalz durch Ersetzen des Kaliumhydroxyds durch die äquivalente Menge Natriumhydroxyd hergestellt. Statt Äthylalkohol wird Methylalkohol der wäßrigen Lösung durch Einlaufen hinzugefiigt, Die Ausbeute ist fast quantitativ. Eine Analyse des Salzes ergibt: HO#Hg#NH#SOg#Na#H,O berechnet: gefunden: Hg . . . . . . . . . . 56,72% 56,9% N . . ......... 3,96% 4,9% S ............ 9,05% 9,3% Na .......... 6,5 0/0 6,701, H.O ......... 5,1 0/0 6,001', 3. Entsprechend den vorigen Beispielen wird auch das Lithiumsalz hergestellt. Zur Ausfällung wird Äthyl- oder Propylalkohol verwendet.a: In the same way as in Example i, the sodium salt is also prepared by replacing the potassium hydroxide with the equivalent amount of sodium hydroxide. Instead of ethyl alcohol, methyl alcohol is added to the aqueous solution by running it in. The yield is almost quantitative. An analysis of the salt gives: HO # Hg # NH # SOg # Na # H, O calculated: found: Ed. . . . . . . . . . 56.72% 56.9% N . ......... 3.96% 4.9% S ............ 9.05% 9.3% Well .......... 6.5 0/0 6.701, HO ......... 5.1 0/0 6.001 ', 3. The lithium salt is also prepared according to the previous examples. Ethyl or propyl alcohol is used for precipitation.

Die nach dem neuen Verfahren hergestellten Quecksilberverbindungen zeichnen sich durch eine hohe bakterizide Wirkung aus, so daß man sie z. B. als Desinfektionsmittel und Mittel zur Bekämpfung von tierischen und pflanzlichen Schädlingen verwenden kann.The mercury compounds produced using the new process are characterized by a high bactericidal effect, so that they can be used for. B. as Disinfectants and agents for combating animal and vegetable pests can use.

Claims (2)

PATENTANSPRÜCHE: r. Verfahren zur Herstellung der Alkalisalze der Oxymercurisulfamidsäure aus Sulfamidsäure, Alkalihydroxyden und löslichen Quecksilberverbindungen, dadurch gekennzeichnet, daß die Alkalisalze aus wäßrigen alkalischen Lösungen der Sulfamidsäure und von OOuecksilbersalzen mit Alkoholen gefällt werden. PATENT CLAIMS: r. Process for the preparation of the alkali salts of Oxymercuric sulfamic acid from sulfamic acid, alkali hydroxides and soluble mercury compounds, characterized in that the alkali salts from aqueous alkaline solutions of the Sulphamic acid and of oxy-mercury salts with alcohols are precipitated. 2. Verfahren zur Herstellung haltbarer wäßriger Lösungen der nach Anspruch i hergestellten Alkalisalze der Oxymercurisulfamidsäure durch Lösen derselben in Wasser, dadurch gekennzeichnet, daß die Lösungen zwecks Erhöhung ihrer Haltbarkeit mit Zusätzen löslicher Alkalisalze oder von Alkalihydroxyden versehen werden.2. Procedure for the production of durable aqueous solutions of the alkali salts produced according to claim i of oxymercurisulphamic acid by dissolving it in water, characterized in that that the solutions with the addition of soluble alkali salts in order to increase their shelf life or by alkali hydroxides.
DEK132189D 1933-11-17 1933-11-17 Production of soluble compounds of sulfamic acid with mercury and alkali metals Expired DE607291C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DEK132189D DE607291C (en) 1933-11-17 1933-11-17 Production of soluble compounds of sulfamic acid with mercury and alkali metals

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEK132189D DE607291C (en) 1933-11-17 1933-11-17 Production of soluble compounds of sulfamic acid with mercury and alkali metals

Publications (1)

Publication Number Publication Date
DE607291C true DE607291C (en) 1934-12-21

Family

ID=7247550

Family Applications (1)

Application Number Title Priority Date Filing Date
DEK132189D Expired DE607291C (en) 1933-11-17 1933-11-17 Production of soluble compounds of sulfamic acid with mercury and alkali metals

Country Status (1)

Country Link
DE (1) DE607291C (en)

Similar Documents

Publication Publication Date Title
DE607291C (en) Production of soluble compounds of sulfamic acid with mercury and alkali metals
DE595570C (en) Process for the preparation of aqueous solutions of heavy metal compounds of the aromatic halyl sulfamides
DE544500C (en) Process for the preparation of aliphatic auromercaptocarboxylic acids
AT151657B (en) Process for the preparation of formaldehyde sodium sulfoxylates from arsenobenzene compounds.
AT153203B (en) Process for the preparation of water-soluble mercury compounds.
DE687563C (en) Process for the production of durable solutions of calcium salts
AT102313B (en) Process for the representation of complex gold compounds.
DE854952C (en) Process for the preparation of complex aureomycin compounds
AT120405B (en) Process for the preparation of auromercaptocarboxylic acids.
DE422076C (en) Process for the preparation of salts of nitrogen-halogen-substituted arylsulfonamides
DE575598C (en) Process for the preparation of complex compounds of organic heavy metal mercapto compounds
DE338427C (en) Process for the preparation of addition products of hexamethylenetetramine
DE249726C (en)
DE399904C (en) Process for the production of organic mercury compounds
DE420910C (en) Process for the preparation of double compounds from aliphatic amino acids and inorganic alkali salts
DE630404C (en) Disinfectants
DE462201C (en) Water-soluble preparation for the production of an alkali hypochlorite solution
AT137670B (en) Process for the representation of organic mercury bonds.
AT155316B (en) Process for the preparation of formaldehyde sodium sulfoxylates from arsenobenzene compounds.
DE667844C (en) Process for the preparation of amino-substituted arsenobenzene-formaldehyde bisulfite compounds
DE558752C (en) Process for the production of neutral complex antimony salts
DE670743C (en) Disinfectants
DE1542836C (en) Use of substituted benzo 2 thia 1,3 diazinon (4) 2,2 dioxides as herbicides
DE531222C (en) Process for the preparation of bismuth dithioglycolic acid and its salts
AT151959B (en) Process for the purification of crude 4,4'-dioxy-3,3'-diaminoarsenobenzene.